ARKOLEVURA

Informació principal

  • Denominació comercial:
  • ARKOLEVURA SACCHAROMYCES BOULARDII 50 cápsulas
  • formulario farmacéutico:
  • Cápsulas
  • Vía de administración:
  • Oral
  • Utilitza per:
  • Humans
  • Tipo de medicina:
  • medicament al·lopàtic

Documents

Localització

  • Disponible en:
  • ARKOLEVURA SACCHAROMYCES BOULARDII 50 cápsulas
    Andorra
  • Idioma:
  • català

Altres dades

Estat

  • Font:
  • CedimCat - Centre d'Informació de Medicaments de Catalunya
  • Número d'autorització:
  • 153541
  • última actualització:
  • 25-05-2018

Prospecte: composició, indicacions, interacció, posologia, embaràs, lactància, reaccions adverses

ARKOLEVURA SACCHAROMYCES

BOULARDII 50 cápsulas

saccharomyces boulardii

Indicacions

Medicament que regenera la flora normal de l'intestí.

Consideracions

Prengui les càpsules senceres, sense obrir ni mastegar, empassant-les amb ajuda d'un got d'aigua.

Si no pot empassar les càpsules senceres, pot obrir-les acuradament i barrejar el seu contingut amb algun

suc de fruites, iogurt o algun aliment tou tebi (a menys de 30 ºC).

És millor que prengui aquest medicament amb l'estómac buit (1 hora abans dels menjars o 2 hores

després).

Prengui aquest medicament en aixecar-se.

Avisi el seu metge si pateix intolerància a alguns sucres.

Aquest medicament modifica l'acció d'altres fàrmacs, NO prengui altres medicaments sense consultar

abans al seu metge o farmacèutic.

És possible que el seu metge li recomani una dieta especial, que convé seguir per augmentar l'eficàcia

d'aquest medicament.

Mentre prengui aquest medicament procuri beure gran quantitat d'aigua i altres líquids, tret que el seu

metge li indiqui el contrari.

Efectes adversos

Si vostè segueix la pauta indicada, no solen aparèixer efectes adversos.

Posologia

Prengui 2 càpsules 1 hora abans de l'esmorzar, del dinar i del sopar.

VIA ORAL.

8-3-2019

Safety and efficacy of Actisaf® Sc47 (Saccharomyces cerevisiae CNCM I‐4407) as a feed additive for cattle for fattening, dairy cows, weaned piglets and sows

Safety and efficacy of Actisaf® Sc47 (Saccharomyces cerevisiae CNCM I‐4407) as a feed additive for cattle for fattening, dairy cows, weaned piglets and sows

Published on: Thu, 07 Mar 2019 Following a request from the European Commission, the EFSA Panel on Additives and Products or Substances used in Animal Feed (FEEDAP) was asked to deliver a scientific opinion on the safety and efficacy of Actisaf® Sc47 for dairy cows, cattle for fattening, weaned piglets and sows when used as a zootechnical additive. Actisaf® Sc47 consists of viable cells of a strain Saccharomyces cerevisiae and is marketed in three formulations. The FEEDAP Panel considers that the three ...

Europe - EFSA - European Food Safety Authority EFSA Journal

12-1-2019

Assessment of the application for renewal of authorisation of selenomethionine produced by Saccharomyces cerevisiae NCYC R397 for all animal species

Assessment of the application for renewal of authorisation of selenomethionine produced by Saccharomyces cerevisiae NCYC R397 for all animal species

Published on: Fri, 11 Jan 2019 The Panel on Additives and Products or Substances used in Animal Feed (FEEDAP) was asked to deliver a scientific opinion on the application for renewal of authorisation of organic form of selenium produced by Saccharomyces cerevisiae NCYC R397 (Alkosel®) for all animal species. The FEEDAP Panel has delivered two opinions (on 2007 and 2016) on the safety and efficacy of the additive. The additive is characterised as organic selenium mainly selenomethionine (63%); it was ini...

Europe - EFSA - European Food Safety Authority EFSA Journal

28-9-2018

Peer review of the pesticide risk assessment of the active substance ABE‐IT 56 (components of lysate of Saccharomyces cerevisiae strain DDSF623)

Peer review of the pesticide risk assessment of the active substance ABE‐IT 56 (components of lysate of Saccharomyces cerevisiae strain DDSF623)

Published on: Thu, 27 Sep 2018 00:00:00 +0200 The conclusions of EFSA following the peer review of the initial risk assessments carried out by the competent authority of the rapporteur Member State, France, for the pesticide active substance ABE‐IT 56 (components of lysate of Saccharomyces cerevisiae strain DDSF623) are reported. The context of the peer review was that required by Regulation (EC) No 1107/2009 of the European Parliament and of the Council. The conclusions were reached on the basis of the...

Europe - EFSA - European Food Safety Authority Publications

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